FDA 510(k) clearances — page 1612
clearances on record, most recent first.
Clearances — page 1612
161,101–161,200 of 175,890- K820970 — RETRIEVAL FORCEPS W/RATTOOTHED JAWS
- K820972 — BIOPSY FORCEPS W/OVAL CUPS
- K820975 — GILCHEM ACID PHOSPHATASE REAGENT
- K820976 — GIL CHEM MAGNESIUM REAGENT
- K820980 — BIOPSY FORCEPS W/OVAL CUP & NEEDLE
- K820983 — HOT BIOPSY FORCEPS W/ROUND CUPS
- K820991 — KENZ-GELECT GEL PAD
- K821000 — ENZYMUNE-TEST DIGOXIN
- K821016 — QUADRUPLE JOGGER EXERCISER
- K821019 — PHOSPHATE BUFFERED CLYCEROL MOUNTING FLU
- K821028 — FINGER COTS
- K821036 — ENTERNAL SOLUTION ADMIN. SET
- K821045 — NON CONDUCTIVE PEDIATRIC ANES. FACE
- K827177 — LTRASONIC SCANNER U.S. ALOKA SSD-500
- K827291 — MODEL PUP II AND MINI-NEBULIZER
- K820784 — CLINIC 2000 MODEL MULTI-FRECODYN DEVICE
- K813224 — CERAVITAL CERAMIC EAR CANAL WALL PROSTH
- K820014 — HOLTER ECG SCANNER
- K820159 — PRESSURE INFUSER
- K820160 — HOLLISTER WOUND EXUDATE ABSORBER
- K820289 — ANTHROSCOPIC SURGICAL TABLE
- K820325 — STERICIDAL
- K820615 — DACOMED SNAP-GAUGE
- K820661 — MICRO-AIRE DISPOSABLE MINI & MAXI LAVAG
- K820702 — IL 7F FLOW DIRECTOR THERMAL DILU. CATH
- K820761 — PALM BEACH SEATING SYSTEM
- K820823 — MULTIPLE, MODEL #17
- K820860 — VOLUMETRIC PUMP CASSETTE W/ATTACHED SET
- K820876 — MODEL 3854 ELECTRODE
- K820896 — VENTREX 125I ANTI-IGE ALLERGY ISOTOPE
- K820898 — VASCULAB SPECTRUM ANALYZER #SP25
- K820904 — EKG TELEPHONE CONVERTER
- K820914 — EMEM POWERED MEDIUM
- K820915 — MEM AUTOCLAVABLE MEDIUM
- K820916 — D-MEM-HIGH GLUCOSE-POWDERED MEDIUM
- K820917 — L-15 POWDERED MEDIUM
- K820918 — HMEM POWDERED MEDIUM
- K820919 — EARLE'S-199 POWDERED MEDIUM
- K820920 — MCCOY'S 5A POWDERED MEDIUM
- K820921 — D-MEM-LOW GLUCOSE-POWDERED MEDIUM
- K820922 — HAMS F-10 POWDERED MEDIUM
- K820923 — DULBECCO'S PBS POWDER
- K820924 — HAMS F-12 POWDERED MEDIUM
- K820925 — H - BME POWDERED MEDIUM
- K820926 — E-BME POWDERED MEDIUM
- K820927 — HBS POWDER
- K820928 — EBS POWDER
- K820929 — RPMI-164POWDERED MEDIUM
- K820930 — FISCHER'S POWDERED MEDIUM
- K820931 — HANK'S 199 POWDERED MEDIUM
- K820963 — PATIENT PAL I.V. WALKER
- K821009 — BATHTUB GRAB BAR
- K821010 — BATHTUB TRANSFER BENCH
- K821402 — LIGHT WEIGHT ALUMINUM CANES
- K827284 — MODEL SSD-119
- K827285 — MODEL SSD-710
- K827288 — MLX LATERAL IMAGING SYSTEM
- K827289 — DIGITAL RADIOGRAPHY SYSTEM
- K820962 — COTTON SWABS
- K820501 — ORX DENT-AIDE DENTAL EMERGENCY KIT
- K820248 — RODDER VOLUME VENTILATOR
- K820369 — SUCTION CATHETERS & KITS
- K820370 — NASAL OXYGEN CATHETER
- K820452 — PHONOTRACE 2000
- K820487 — IMPLANTIBLE SUTURE SLEEVE
- K820499 — FITC ANTI-RABIES MONOCLONAL GLOBULIN
- K820746 — NEWPORT VENTILATOR MODEL E100
- K820760 — LH RADIOIMMUNOASSAY TEST SYSTEM
- K820769 — GAMBRO LUNDIA 10 3N PARALLEL FLOW DIAL
- K820839 — CULTURE MEDIA, SINGLE BIOCHEM. TEST
- K820840 — CULTURE MEDIA, GENERAL NUTRIENT BROTH
- K820841 — CULTURE MEDIA, MULTIPLE BIOCHEMICAL
- K820842 — CULTURE MEDIA, NON-SELECTIVE/DIFFER
- K820843 — CULTURE MEDIA SELECTIVE BROTH
- K820844 — CULTURE MEDIA, SELECTIVE & DIFFERENTIAL
- K820845 — DULTURE MEDIA, SELECTIVE & NON-DIFFER
- K820846 — ANTIMICROBIAL SUSCEP. TEST, MUELLER
- K820847 — ISOLATION OF PATHOGENIC NEISSERIA
- K820848 — BLUE RIDGE SHEEP BLOOD
- K820849 — BLUE RIDGE RABBIT BLOOD
- K820859 — COAXIAL DUAL FLOW CATHETER
- K820863 — MEDIA FOR IN-VITRO DIAGNOSTIC USE
- K820873 — CORNING CERTAIN TM
- K820879 — ENZYME-TEST TBC T4 UPTAKE
- K820880 — SERALYZER CK REAGENT STRIPS
- K820886 — THYROXINE T4 KIT
- K820935 — MODEL 5866-26 LEAD ADAPTER KIT
- K820961 — INCONTINENCE PAD OR ADULT DIAPER
- K820964 — WHEELCHAIR PAL
- K820965 — DISSCAP 140
- K820966 — DISSCAP 110
- K820973 — ENDOSCOPIC INJECTION NEEDLE
- K827296 — POLYSONIC ULTRASOUND LOTION
- K813223 — DISPOSABLE PLASTIC SYRINGE W/NEEDLE
- K820384 — GLASS SYRINGES, DRUG, LUER LOCK
- K820477 — ALGORITHM OF THE ARRHYTHMIA MON. SYS
- K820516 — ARTERIAL CANALIZATION DEVICE
- K820599 — AUTOSPIROMETER HI-498
- K820645 — INFANT MONITOR
- K820657 — PULSE GENERATOR 678 B
Data sourced from openFDA. This site is unofficial and independent of the FDA.